ABSTRACT
Retinoids display anti-tumour activity on various cancer cells and therefore have been used as important therapeutic agents. However, adverse side effects and RA (retinoic acid) resistance limit further development and clinical application of retinoid-based therapeutic agents. We report in the present paper the identification of a natural marine product that activates RARs (RA receptors) with a chemical structure distinct from retinoids by high-through put compound library screening. Luffariellolide was uncovered as a novel RAR agonist by inducing co-activator binding to these receptors in vitro, further inhibiting cell growth and regulating RAR target genes in various cancer cells. Structural and molecular studies unravelled a unique binding mode of this natural ligand to RARs with an unexpected covalent modification on the RAR. Functional characterization further revealed that luffariellolide displays chemotherapeutic potentials for overcoming RA resistance in colon cancer cells, suggesting that luffariellolide may represent a unique template for designing novel non-retinoid compounds with advantages over current RA drugs.
Revealing a natural marine product as a novel agonist for retinoic acid receptors with a unique binding mode and inhibitory effects on cancer cells
Riferimento:
Biochem J. 2012 Aug 15;446(1):79-87.
Autori:
Wang S, Wang Z, Lin S, Zheng W, Wang R, Jin S, Chen J, Jin L, Li Y.
Fonte:
Biochem J. 2012 Aug 15;446(1):79-87.
Anno:
2012
Azione:
luffariellolide, un prodotto marino naturale che attiva i recettori RA, mostra potenzialità chemioterapiche per superare la resistenza nelle cellule tumorali del colon all'acido retinoico (RA).
Target:
RA-Luffariellolide/cancro del colon.
Sostanze: